Vapr Vue

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name: VAPR VUE FDA UDI
Generic Name: Electrosurgical system generator FDA UDI
Device Name: VAPR VUE Generator REUSABLE FDA UDI
Model / Reference: 225024 FDA UDI
Description: VAPR VUE Generator REUSABLE FDA UDI

Identifiers

Catalog Number: 225024 FDA UDI
Primary DI / UDI-DI: 10886705009121 FDA UDI
FDA Product Code: GEI FDA UDI
HRX FDA UDI
GMDN Term: Electrosurgical system generator FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4400 FDA UDI
888.1100 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Electrosurgical system generator

Vapr Vue by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical system generator.

Cook — COOK INCORPORATED · Class II
LEEP PRECISION™ Generator — CooperSurgical, Inc. · Class II
AEXTM — MEDTRONIC, INC. · Class II
Cook — COOK INCORPORATED · Class II
Endovapor® — JOIMAX, INC. · Class II
WEREWOLF — Smith & Nephew, Inc. · Class II
PerFect TCS — Coltene/Whaledent Inc. · Class II
INTELLIO SHIFT — Smith & Nephew, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Medos International Sàrl

Sources (1)

FDA UDI 08ebfe93-c147-4893-bb36-4fca561d92e3 36 fields · synced May 30, 2026